Canonical Allele Identifier: CA8729399
Gene: PRKAR1A HGNC NCBI

Linked Data

dbSNP Id: rs779359790

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.68529017_68529052del , CM000679.2:g.68529017_68529052del GRCh38
NC_000017.10:g.66525158_66525193del , CM000679.1:g.66525158_66525193del GRCh37
NC_000017.9:g.64036753_64036788del NCBI36
NG_007093.3:g.120395_120430del , LRG_514:g.120395_120430del

Transcript Alleles

HGVS Amino-acid change
ENST00000588188.7:c.891+26_891+61del
ENST00000711037.1:c.891+26_891+61del
ENST00000585427.6:c.891+26_891+61del
ENST00000585981.6:c.891+26_891+61del
ENST00000588178.6:c.891+26_891+61del
ENST00000589017.6:c.891+26_891+61del
ENST00000589480.6:c.891+26_891+61del
ENST00000592800.6:c.891+26_891+61del
ENST00000686019.1:n.1036_1071del
ENST00000689501.1:n.3083+26_3083+61del
ENST00000691392.1:n.1858+26_1858+61del
ENST00000589228.6:c.891+26_891+61del
ENST00000358598.6:c.891+26_891+61del
ENST00000392710.8:c.*506+26_*506+61del
ENST00000392711.5:c.891+26_891+61del
ENST00000536854.6:c.891+26_891+61del
ENST00000585907.1:n.439+26_439+61del
ENST00000586397.5:c.891+26_891+61del
ENST00000586541.5:c.303+26_303+61del
ENST00000588188.6:c.891+26_891+61del
ENST00000589228.5:c.891+26_891+61del
ENST00000592800.5:c.301+26_301+61del
NM_001276289.1:c.891+26_891+61del
NM_001276290.1:c.891+26_891+61del
NM_001278433.1:c.891+26_891+61del
NM_002734.4:c.891+26_891+61del , LRG_514t1:c.891+26_891+61del
NM_212471.2:c.891+26_891+61del
NM_212472.2:c.891+26_891+61del , LRG_514t2:c.891+26_891+61del
XM_011524983.1:c.891+26_891+61del
XM_011524984.1:c.891+26_891+61del
XM_011524985.1:c.891+26_891+61del
XM_011524983.3:c.891+26_891+61del
XM_011524984.3:c.891+26_891+61del
XM_011524985.3:c.891+26_891+61del
NM_001369389.1:c.891+26_891+61del
NM_001369390.1:c.891+26_891+61del
NM_002734.5:c.891+26_891+61del
NM_001276289.2:c.891+26_891+61del
NM_001278433.2:c.891+26_891+61del
NM_212471.3:c.891+26_891+61del